| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:32392150-32392650 | Common:5; Rare:96 | ||||
| chr3:32502355-32502510 | Common:1; Rare:43 | ||||
| chr3:32502787-32502941 | Rare:40 | ||||
| chr3:32569990-32570360 | Common:3; Rare:127 | ||||
| chr3:32570771-32571032 | Common:1; Rare:115 | ||||
| chr3:32685024-32685392 | Rare:112 | ||||
| chr3:33096381-33096781 | Common:5; Rare:118 | ||||
| chr3:33096726-33096878 | Rare:79 | ||||
| chr3:33097095-33097376 | Common:3; Rare:82; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:33113630-33114260 | Common:3; Rare:202; Clinvar:8; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr3:33114472-33114647 | Common:1; Rare:67; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr3:33115243-33115643 | Common:2; Rare:87 | ||||
| chr3:33218650-33219080 | Common:5; Rare:136 | ||||
| chr3:33277294-33277522 | Common:3; Rare:66 | ||||
| chr3:33278109-33278509 | Common:1; Rare:76 |